United States · FDA National Drug Code directory

MICONAZOLE Nitrate 2% Cream ANTIFUNGAL

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
69396-014_4e55e0bf-9e9d-d877-e063-6294a90a9d59
Product NDC
69396-014
Form
CREAM
Composition / generic term
MICONAZOLE NITRATE
Labeler
Trifecta Pharmaceuticals Usa Llc
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20160322
Source listing expiry
20271231

Source-listed ingredients

  • MICONAZOLE NITRATE — 2 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 118.3 g in 1 TUBE (69396-014-04) · 69396-014-04
  • 15 g in 1 TUBE (69396-014-05) · 69396-014-05
  • 1 TUBE in 1 BOX (69396-014-20) / 30 g in 1 TUBE · 69396-014-20
  • 3 TUBE in 1 BOX (69396-014-33) / 30 g in 1 TUBE · 69396-014-33
  • 4 TUBE in 1 BOX (69396-014-44) / 30 g in 1 TUBE · 69396-014-44
  • 6 TUBE in 1 BOX (69396-014-66) / 30 g in 1 TUBE · 69396-014-66

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →